Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss

• Κύριοι συγγραφείς: Marjan MASOUDI (Συγγραφέας), Najmeh AHANGARI (Συγγραφέας), Ali Akbar POURSADEGH ZONOUZI (Συγγραφέας), Ahmad POURSADEGH ZONOUZI (Συγγραφέας), Azim NEJATIZADEH (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Tehran University of Medical Sciences, 2016-05-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

Background: Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common hereditary form of deafness, and exhibits a great deal of genetic heterogeneity. So far, more than seventy various DFNB loci have been mapped for ARNSHL by linkage analysis. The contribution of three common DFNB l...